Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
399 0 1 1.5E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
272 0 1 1.9E-03 0 0
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
264 0 1 1.9E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis
237 0 1 2.1E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
219 0 1 2.1E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
194 0 1 2.3E-03 0 0
Malformations of Cortical Development, Group II
180 0 1 2.3E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 2.4E-03 0 0
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement
160 0 1 2.4E-03 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia
152 0 1 2.5E-03 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia
142 0 1 2.6E-03 0 0
Platelet Component Distribution Width Measurement
134 0 1 2.6E-03 0 0
CUI: C0233565
Disease: Bradykinesia
Bradykinesia
133 0 1 2.6E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria
129 0 1 2.6E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary
123 0 1 2.7E-03 0 0
CUI: C0476254
Disease: Dyslexia
Dyslexia
118 0 1 2.7E-03 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness
117 0 1 2.7E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination
112 0 1 2.8E-03 0 0
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
109 0 1 2.8E-03 0 0
CUI: C1839758
Disease: Narrow forehead
Narrow forehead
106 0 1 2.8E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology
104 0 1 2.8E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin
101 0 1 2.8E-03 0 0
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence
100 0 1 2.9E-03 0 0
CUI: C4551488
Disease: Bifid uvula
Bifid uvula
97 0 1 2.9E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis
95 0 1 2.9E-03 0 0